Evidence map›Paper›PMID 26295585›Full record

SynthesisPloS one2015

Creatinine Change on Vasoconstrictors as Mortality Surrogate in Hepatorenal Syndrome: Systematic Review & Meta-Analysis.

Justin M Belcher, Steven G Coca, Chirag R Parikh

Open access · goldAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 40% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 16 citations in OpenAlex.

  1. Reduction in acute kidney injury stage predicts survival in patients with type-1 hepatorenal syndrome.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2020
    Trial
  2. Management of hepatorenal syndrome in liver cirrhosis: a recent update.Therapeutic advances in gastroenterology · 2022
    Review
  3. Article
  4. Terlipressin effect on hepatorenal syndrome: Updated meta-analysis of randomized controlled trials.JGH open : an open access journal of gastroenterology and hepatology · 2021
    Article
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Justin M BelcherProgram of Applied Translational Research, Yale University School of Medicine, New Haven, CT, United States of America; Section of Nephrology, Yale University School of Medicine, New Haven, CT, United States of America; Clinical Epidemiology Research Center, VAMC, West Haven, CT, United States of America.
Steven G CocaProgram of Applied Translational Research, Yale University School of Medicine, New Haven, CT, United States of America; Section of Nephrology, Yale University School of Medicine, New Haven, CT, United States of America; Clinical Epidemiology Research Center, VAMC, West Haven, CT, United States of America.
Chirag R ParikhProgram of Applied Translational Research, Yale University School of Medicine, New Haven, CT, United States of America; Section of Nephrology, Yale University School of Medicine, New Haven, CT, United States of America; Clinical Epidemiology Research Center, VAMC, West Haven, CT, United States of America.
Yale University · US

Funding

Mentoring Program for Translational and Patient Oriented Research in AKIK24DK090203 · NIDDK · YALE UNIVERSITY · PI PARIKH, CHIRAG R · 2012 to 2016
$896k
NIDDK NIH HHS K24 DK090203NIDDK NIH HHS K24-DK090203
6 · The paper itself

Abstract

BACKGROUND AND

aimsHepatorenal syndrome is a severe complication of cirrhosis and associates with significant mortality. Vasoconstrictor medications improve renal function in patients with hepatorenal syndrome. However, it is unclear to what extent changes in serum creatinine during treatment may act as a surrogate for changes in mortality. We have performed a meta-analysis of randomized trials of vasoconstrictors assessing the association between changes in serum creatinine, taken as a continuous variable, and mortality, both while on treatment and during the follow-up period for survivors.

methodsThe electronic databases of PubMed, Web of Science and Embase were searched for randomized trials evaluating the efficacy of vasoconstrictor therapy for treatment of HRS type 1 or 2. The relative risk (RR) for mortality was calculated against delta creatinine. The proportion of treatment effect explained (PTE) was calculated for delta creatinine.

resultsSeven trials enrolling 345 patients were included. The correlation between delta creatinine and ln (RR) was moderately good (R2 = 0.61). The intercept and parameter estimate indicated a fall in creatinine while on treatment of 1 mg/dL resulted in a 27% reduction in RR for mortality compared to the control arm. In patients surviving the treatment period, a fall in creatinine while on treatment of 1 mg/dL resulted in a 16% reduction in RR for post-treatment mortality during follow-up. The PTE of delta creatinine for overall mortality was 0.91 and 0.26 for post-treatment mortality.

conclusionsChanges in serum creatinine in response to vasoconstrictor therapy appear to be a valid surrogate for mortality, even in the period following the completion of treatment.

Indexed as

BiomarkersCreatinineHepatorenal SyndromeHumansLiver CirrhosisLypressinRandomized Controlled Trials as TopicRiskSurvival AnalysisVasoconstrictor AgentsBiomarkersCreatinineLypressinVasoconstrictor Agents

Identifiers

PMID26295585
PMCPMC4546623
OpenAlexW1883254629

What OpenQuestion holds

Textmetadata
LicenceCC0
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.